Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40443254-40443491 | Common:1; Rare:75 | ||||
chr17:41528269-41528550 | Common:1; Rare:66; Clinvar:1 | ||||
chr17:41688656-41689069 | Common:3; Rare:166 | ||||
chr17:41689277-41689627 | Common:3; Rare:128 | ||||
chr17:41785028-41785471 | Common:3; Rare:102 | ||||
chr17:41785951-41786045 | Rare:18 | ||||
chr17:41786673-41787053 | Common:2; Rare:94 | ||||
chr17:41812567-41812772 | Common:3; Rare:43; Clinvar:2 | ||||
chr17:41812801-41813270 | Rare:130; Clinvar:7 | ||||
chr17:41818084-41818545 | Common:1; Rare:159; Clinvar:8; Clinvar (benign):2 | ||||
chr17:41835974-41836111 | Common:2; Rare:38 | ||||
chr17:41836152-41836339 | Common:1; Rare:49 | ||||
chr17:41918881-41919321 | Common:3; Rare:161; Clinvar:1 | ||||
chr17:41930484-41930676 | Rare:57 | ||||
chr17:42016944-42017048 | Rare:16 |